FDA Inspection 622929 — Invivo Corporation

Invivo Corporation — FEI 1051786

The FDA completed an inspection of Invivo Corporation on Oct 14, 2009 in Orlando, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 14, 2009
Fiscal Year
2010
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Orlando, FL (United States)

Citations

IDCFRDescription
369621 CFR 820.100(b)Documentation